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Periphilin self-association underpins epigenetic silencing by the HUSH complex

Prigozhin, Daniil M (author)
Douse, Christopher H (author)
Lund University,Lunds universitet,LUCC: Lunds universitets cancercentrum,Övriga starka forskningsmiljöer,Epigenetik och kromatindynamik,Forskargrupper vid Lunds universitet,LUCC: Lund University Cancer Centre,Other Strong Research Environments,Epigenetics and Chromatin Dynamics,Lund University Research Groups,University of Cambridge
Albecka, Anna (author)
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Tchasovnikarova, Iva A (author)
Timms, Richard T (author)
Oda, Shun-Ichiro (author)
Adolf, Frank (author)
Freund, Stefan M V (author)
Maslen, Sarah (author)
Lehner, Paul J (author)
Modis, Yorgo (author)
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 (creator_code:org_t)
2020-09-25
2020
English.
In: Nucleic Acids Research. - : Oxford University Press (OUP). - 1362-4962 .- 0305-1048. ; 48:18, s. 10313-10328
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Transcription of integrated DNA from viruses or transposable elements is tightly regulated to prevent pathogenesis. The Human Silencing Hub (HUSH), composed of Periphilin, TASOR and MPP8, silences transcriptionally active viral and endogenous transgenes. HUSH recruits effectors that alter the epigenetic landscape and chromatin structure, but how HUSH recognizes target loci and represses their expression remains unclear. We identify the physicochemical properties of Periphilin necessary for HUSH assembly and silencing. A disordered N-terminal domain (NTD) and structured C-terminal domain are essential for silencing. A crystal structure of the Periphilin-TASOR minimal core complex shows Periphilin forms an α-helical homodimer, bound by a single TASOR molecule. The NTD forms insoluble aggregates through an arginine/tyrosine-rich sequence reminiscent of low-complexity regions from self-associating RNA-binding proteins. Residues required for TASOR binding and aggregation were required for HUSH-dependent silencing and genome-wide deposition of repressive mark H3K9me3. The NTD was functionally complemented by low-complexity regions from certain RNA-binding proteins and proteins that form condensates or fibrils. Our work suggests the associative properties of Periphilin promote HUSH aggregation at target loci.

Subject headings

NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)

Keyword

Antigens, Neoplasm/chemistry
Crystallography, X-Ray
DNA Transposable Elements/genetics
Epigenesis, Genetic/genetics
Gene Silencing
Humans
Nuclear Proteins/chemistry
Phosphoproteins/chemistry
Protein Aggregates/genetics
Protein Binding/genetics
Protein Conformation, alpha-Helical
Protein Domains/genetics
RNA-Binding Proteins/chemistry
Transcription, Genetic
Viruses/genetics

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art (subject category)
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